LDH info

Canonical Allele Identifier: CA16336380
Gene: CA8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10098647

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192640T>C , CM000670.2:g.60192640T>C GRCh38
NC_000008.10:g.61105199T>C , CM000670.1:g.61105199T>C GRCh37
NC_000008.9:g.61267753T>C NCBI36
NG_023193.1:g.93756A>G
NG_023193.2:g.93756A>G

Transcript Alleles

HGVS Amino-acid change
NM_004056.4:c.*36-2655A>G VV NP_004047.3:p.=
XM_011517586.1:c.*36-2655A>G XP_011515888.1:p.=
NM_001321839.1:c.*36-2655A>G VV NP_001308768.1:p.=
NM_004056.5:c.*36-2655A>G VV NP_004047.3:p.=
NR_135821.1:n.1235-2655A>G
XM_017013818.1:c.*36-2655A>G XP_016869307.1:p.=
NM_004056.6:c.*36-2655A>G VV MANE Preferred NP_004047.3:p.=
ENST00000317995.4:c.*36-2655A>G ENSP00000314407.4:p.=